Salih MA - Search Results

1

Genomic and phenotypic delineation of congenital microcephaly.

Shaheen R, Maddirevula S, Ewida N, Alsahli S, Abdel-Salam GMH, Zaki MS, Tala SA, Alhashem A, Softah A, Al-Owain M, Alazami AM, Abadel B, Patel N, Al-Sheddi T, Alomar R, Alobeid E, Ibrahim N, Hashem M, Abdulwahab F, Hamad M, Tabarki B, Alwadei AH, Alhazzani F, Bashiri FA, Kentab A, Şahintürk S, Sherr E, Fregeau B, Sogati S, Alshahwan SAM, Alkhalifi S, Alhumaidi Z, Temtamy S, Aglan M, Otaify G, Girisha KM, Tulbah M, Seidahmed MZ, Salih MA, Abouelhoda M, Momin AA, Saffar MA, Partlow JN, Arold ST, Faqeih E, Walsh C, Alkuraya FS. Shaheen R, et al. Among authors: salih ma. Genet Med. 2019 Mar;21(3):545-552. doi: 10.1038/s41436-018-0140-3. Epub 2018 Sep 14. Genet Med. 2019. PMID: 30214071 Free PMC article.

2

Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?

Seidahmed MZ, Sunada Y, Ozo CO, Hamid F, Campbell KP, Salih MA. Seidahmed MZ, et al. Among authors: salih ma. Neuropediatrics. 1996 Dec;27(6):305-10. doi: 10.1055/s-2007-973799. Neuropediatrics. 1996. PMID: 9050048

3

Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome.

Seidahmed MZ, Rooney DE, Salih MA, Basit OB, Shaheed MM, Abdullah MA, Abomelha A. Seidahmed MZ, et al. Among authors: salih ma. Am J Med Genet. 1999 Jul 16;85(2):185-8. doi: 10.1002/(sici)1096-8628(19990716)85:2<185::aid-ajmg16>3.0.co;2-w. Am J Med Genet. 1999. PMID: 10406675 Review.

4

Determination of urinary S-sulphocysteine, xanthine and hypoxanthine by liquid chromatography-electrospray tandem mass spectrometry.

Rashed MS, Saadallah AA, Rahbeeni Z, Eyaid W, Seidahmed MZ, Al-Shahwan S, Salih MA, Osman ME, Al-Amoudi M, Al-Ahaidib L, Jacob M. Rashed MS, et al. Among authors: salih ma. Biomed Chromatogr. 2005 Apr;19(3):223-30. doi: 10.1002/bmc.439. Biomed Chromatogr. 2005. PMID: 15558695

5

Brain stem and cerebellar findings in Joubert syndrome.

Alorainy IA, Sabir S, Seidahmed MZ, Farooqu HA, Salih MA. Alorainy IA, et al. Among authors: salih ma. J Comput Assist Tomogr. 2006 Jan-Feb;30(1):116-21. doi: 10.1097/01.rct.0000191681.05473.13. J Comput Assist Tomogr. 2006. PMID: 16365585

6

Perinatal stroke in Saudi children. Clinical features and risk factors.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Al-Nasser MN. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S35-40. Saudi Med J. 2006. PMID: 16532129

7

Infectious and inflammatory disorders of the circulatory system as risk factors for stroke in Saudi children.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Gadelrab MO, Alorainy IA, Hassan HH, Zahraa JN. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S41-52. Saudi Med J. 2006. PMID: 16532131

8

Congenital and genetic cerebrovascular anomalies as risk factors for stroke in Saudi children.

Salih MA, Murshid WR, Zahraa JN, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Tjan GT. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S53-60. Saudi Med J. 2006. PMID: 16532132

9

Cardiac diseases as a risk factor for stroke in Saudi children.

Salih MA, Al-Jarallah AS, Abdel-Gader AG, Al-Jarallah AA, Al-Saadi MM, Kentab AY, Alorainy IA, Hassan HH. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S61-8. Saudi Med J. 2006. PMID: 16532133

10

Moyamoya syndrome as a risk factor for stroke in Saudi children. Novel and usual associations.

Salih MA, Murshid WR, Al-Salman MM, Abdel-Gader AG, Al-Jarallah AA, Alorainy IA, Hassan HH, Kentab AY, Van Maldergem L, Othman SA, El-Desouki MI, Elgamal EA. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S69-80. Saudi Med J. 2006. PMID: 16532134

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